Evidence map›Paper›PMID 30054757›Full record

ReviewWorld journal of microbiology & biotechnology2018

Heterologous production of resveratrol in bacterial hosts: current status and perspectives.

A Braga, P Ferreira, J Oliveira, I Rocha, N Faria

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in World journal of microbiology & biotechnology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 44 citations in OpenAlex.

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  7. Modular engineering ofSynthetic and systems biotechnology · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

A BragaCentre of Biological Engineering, University of Minho, Campus de Gualtar, 4710-057, Braga, Portugal. abraga@deb.uminho.pt.
P FerreiraCentre of Biological Engineering, University of Minho, Campus de Gualtar, 4710-057, Braga, Portugal.
J OliveiraCentre of Biological Engineering, University of Minho, Campus de Gualtar, 4710-057, Braga, Portugal.
I RochaCentre of Biological Engineering, University of Minho, Campus de Gualtar, 4710-057, Braga, Portugal.
N FariaCentre of Biological Engineering, University of Minho, Campus de Gualtar, 4710-057, Braga, Portugal.
University of Minho · PT

Funding

COMPETE 2020 POCI-01-0145-FEDER-006684European Regional Development Fund NORTE-01-0145-FEDER-000004European Union Framework Program 7 Project No. FP7- 613793Portuguese Foundation for Science and Technology UID/BIO/04469 unit
6 · The paper itself

Abstract

The polyphenol resveratrol (3,5,4'-trihydroxystilbene) is a well-known plant secondary metabolite, commonly used as a medical ingredient and a nutritional supplement. Due to its health-promoting properties, the demand for resveratrol is expected to continue growing. This stilbene can be found in different plants, including grapes, berries (blackberries, blueberries and raspberries), peanuts and their derived food products, such as wine and juice. The commercially available resveratrol is usually extracted from plants, however this procedure has several drawbacks such as low concentration of the product of interest, seasonal variation, risk of plant diseases and product stability. Alternative production processes are being developed to enable the biotechnological production of resveratrol by genetically engineering several microbial hosts, such as Escherichia coli, Corynebacterium glutamicum, Lactococcus lactis, among others. However, these bacterial species are not able to naturally synthetize resveratrol and therefore genetic modifications have been performed. The application of emerging metabolic engineering offers new possibilities for strain and process optimization. This mini-review will discuss the recent progress on resveratrol biosynthesis in engineered bacteria, with a special focus on the metabolic engineering modifications, as well as the optimization of the production process. These strategies offer new tools to overcome the limitations and challenges for microbial production of resveratrol in industry.

Indexed as

BacteriaBacterial ProteinsBiosynthetic PathwaysBiotechnologyGene Expression Regulation, BacterialGenetic EngineeringIndustrial MicrobiologyMalonyl Coenzyme AMetabolic EngineeringMicroorganisms, Genetically-ModifiedResveratrolStilbenesBacterial ProteinsMalonyl Coenzyme AResveratrolStilbenesBacteriaMalonyl-CoAMetabolic engineeringPathway engineeringResveratrol

Identifiers

PMID30054757
OpenAlexW2884178479

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.